A step-economical route to fused 1,2,3-triazoles via an intramolecular 1,3-dipolar cycloaddition between a nitrile and an in situ generated aryldiazomethane.
Mani, Neelakandha S
A step-economical route to fused 1,2,3-triazoles via an intramolecular 1,3-dipolar cycloaddition between a nitrile and an in situ generated aryldiazomethane. [electronic resource] - The Journal of organic chemistry Sep 2014 - 8889-94 p. digital
Publication Type: Journal Article
1520-6904
10.1021/jo5013288 doi
Aldehydes--chemistry
Alkynes--chemistry
Catalysis
Copper--chemistry
Cycloaddition Reaction
Diazomethane--chemistry
Heterocyclic Compounds--chemical synthesis
Molecular Structure
Nitriles--chemistry
Triazoles--chemical synthesis
A step-economical route to fused 1,2,3-triazoles via an intramolecular 1,3-dipolar cycloaddition between a nitrile and an in situ generated aryldiazomethane. [electronic resource] - The Journal of organic chemistry Sep 2014 - 8889-94 p. digital
Publication Type: Journal Article
1520-6904
10.1021/jo5013288 doi
Aldehydes--chemistry
Alkynes--chemistry
Catalysis
Copper--chemistry
Cycloaddition Reaction
Diazomethane--chemistry
Heterocyclic Compounds--chemical synthesis
Molecular Structure
Nitriles--chemistry
Triazoles--chemical synthesis